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Pramlintide · Symlinpen, AC-0137

Peptide · Agonist of amylin receptor · developed by Astrazeneca

Approved FDA, Mar 2005
1 Registered trials

What is Pramlintide?

Pramlintide is a synthetic analog of human amylin, a hormone cosecreted with insulin by pancreatic beta cells. It slows gastric emptying, suppresses glucagon secretion, and increases satiety, thereby reducing postprandial glucose levels. It is used as adjunctive therapy in type 1 and type 2 diabetes patients on mealtime insulin who have not achieved adequate glycemic control.

Summary written with AI from the sources listed at the end of this page.

At a glance

Also known as
Symlinpen, AC-0137, AC-137
Drug type
Peptide
Targets
amylin receptor
Mechanism
Agonist of amylin receptor
Pathways
gastric emptying, glucagon secretion, satiety, glucose homeostasis
Therapy area
Endocrine
Developer
Astrazeneca Ab
In trials of
XERS
FDA status
Approved as Symlinpen (March 16, 2005), NDA021332 · FDA label
UNII
D3FM8FA78T

✅ FDA-approved uses

From the indications section of the FDA label (version of Dec 18, 2019). Read the full label for the exact wording, limitations and safety information.

🧪 Clinical trials

TrialPhaseConditionStatusSponsor
NCT04074317 Phase 2 Diabetes Mellitus, Type 1 Completed XERS

Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.

Conditions studied

Diabetes Mellitus, Type 1Insulin-dependent Diabetes Mellitus

Sources

Updated Oct 3, 2026.

Data: FDA (Drugs@FDA, Purple Book, DailyMed), NIH (NCI Thesaurus, GSRS, RxNorm), ClinicalTrials.gov • Informational purposes only, not medical or investment advice. • All drugs A–Z

This data is for informational purposes only, not investment advice. BioRadar does not provide buy/sell recommendations. Past performance does not guarantee future results. Always do your own due diligence.